Evidence map›Paper›PMID 32244535›Full record

ArticleInternational journal of molecular sciences2020

Alpha-l-Locked Nucleic Acid-Modified Antisense Oligonucleotides Induce Efficient Splice Modulation In Vitro.

Prithi Raguraman, Tao Wang, Lixia Ma, Per Trolle Jørgensen, Jesper Wengel, Rakesh N Veedu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 3 countries.

Prithi RaguramanCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth 6150 Australia.
Tao WangCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth 6150 Australia.
Lixia MaSchool of Statistics, Henan University of Economics and Law, Zhengzhou 450001, China.
Per Trolle JørgensenNucleic Acid Center, Department of Physics and Chemistry and Pharmacy, University of Southern Denmark, M 5230 Odense, Denmark.ORCID 0000-0003-3932-5921
Jesper WengelNucleic Acid Center, Department of Physics and Chemistry and Pharmacy, University of Southern Denmark, M 5230 Odense, Denmark.ORCID 0000-0001-9835-1009
Rakesh N VeeduCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth 6150 Australia.ORCID 0000-0003-2192-9532
Murdoch University · AUUniversity of Southern Denmark · DKHenan University of Economic and Law · CN

Funding

Horizon 2020 810685
6 · The paper itself

Abstract

Alpha-l-Locked nucleic acid (α-l-LNA) is a stereoisomeric analogue of locked nucleic acid (LNA), which possesses excellent biophysical properties and also exhibits high target binding affinity to complementary oligonucleotide sequences and resistance to nuclease degradations. Therefore, α-l-LNA nucleotides could be utilised to develop stable antisense oligonucleotides (AO), which can be truncated without compromising the integrity and efficacy of the AO. In this study, we explored the potential of α-l-LNA nucleotides-modified antisense oligonucleotides to modulate splicing by inducing

Indexed as

AnimalsCell SurvivalExonsMiceMice, Inbred mdxMyoblastsNucleotidesOligonucleotidesOligonucleotides, Antisenselocked nucleic acidNucleotidesOligonucleotidesOligonucleotides, Antisenseantisense oligonucleotidesDMDlocked nucleic acidsα-l-LNA

Identifiers

PMID32244535
PMCPMC7177859
OpenAlexW3014229555

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.